Canonical Allele Identifier: CA1845635292

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647097C= , CM000671.2:g.34647097C=	GRCh38
NC_000009.11:g.34647094C= , CM000671.1:g.34647094C=	GRCh37
NC_000009.10:g.34637094C=	NCBI36
NG_009029.1:g.5460C=
NG_009029.2:g.5509C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000155.4:c.91C= MANE Select	NP_000146.2:p.His31=
ENST00000378842.8:c.91C= MANE Select	ENSP00000368119.4:p.His31=
NM_000155.3:c.91C=	NP_000146.2:p.His31=
NM_001258332.1:c.-112C=	NP_001245261.1:n.-112C=
NM_001258332.2:c.-112C=	NP_001245261.1:n.-112C=
ENST00000378842.7:c.91C=	ENSP00000368119.3:p.His31=
ENST00000450095.6:c.-112C=	ENSP00000401956.2:n.-112C=
ENST00000465543.6:n.430C=
ENST00000468099.2:n.155-24C=
ENST00000472111.5:n.132C=
ENST00000473506.6:c.91C=	ENSP00000432839.2:p.His31=
ENST00000473529.5:n.138C=
ENST00000485531.1:n.84C=
ENST00000487381.5:n.117C=
ENST00000489643.6:n.121C=
ENST00000554085.5:c.91C=	ENSP00000450419.1:p.His31=
ENST00000554139.5:n.144C=
ENST00000554330.5:n.88C=
ENST00000554550.5:c.91C=	ENSP00000451435.1:p.His31=
ENST00000554638.5:n.115C=
ENST00000554897.5:c.91C=	ENSP00000450942.1:p.His31=
ENST00000554944.5:n.121C=
ENST00000555020.5:n.121C=
ENST00000555086.5:n.95C=
ENST00000555214.5:n.100C=
ENST00000556157.1:n.198C=
ENST00000556278.1:c.91C=	ENSP00000451792.1:p.His31=
ENST00000556403.5:n.104C=
ENST00000556494.5:n.123C=
ENST00000557541.5:n.284C=
ENST00000557706.5:n.205C=
ENST00000605275.1:n.629C=
ENST00000691183.1:c.91C=	ENSP00000509954.1:p.His31=